Laminin-1-induced migration of multiple myeloma cells involves the high-affinity 67 kD laminin receptor

被引:0
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作者
I Vande Broek
K Vanderkerken
C De Greef
K Asosingh
N Straetmans
B Van Camp
I Van Riet
机构
[1] Free University Brussels (VUB),Department of Hematology and Immunology
[2] Saint-Luc Hospital,Department of Internal Medicine and Hematology
来源
British Journal of Cancer | 2001年 / 85卷
关键词
multiple myeloma; homing; laminin-1; 67LR; migration; extravasation;
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摘要
The 67 kD laminin receptor (67LR) binds laminin-1 (LN), major component of the basement membrane, with high affinity. In this study, we demonstrated that human multiple myeloma cell lines (HMCL) and murine 5T2MM cells express 67LR. CD38bright+ plasma cells in fresh multiple myeloma (MM) bone marrow (BM) samples showed weaker 67LR expression, but expression increased after direct exposure to a BM endothelial cell line (4LHBMEC). LN stimulated the in vitro migration of 3 HMCL (MM5.1, U266 and MMS.1), primary MM cells and the murine 5T2MM cells. 67LR has been shown to mediate the actions of LN through binding to CDPGYIGSR, a 9 amino acid sequence from the B1 chain of LN. MM cell migration was partially blocked by peptide 11, a synthetic nonapeptide derived from this amino sequence and also by a blocking antiserum against 67LR. Co-injection of peptide 11 with 5T2MM cells in a murine in vivo model of MM resulted in a decreased homing of 5T2MM cells to the BM compartment. In conclusion, LN acts as a chemoattractant for MM cells by interaction with 67LR. This interaction might be important during extravasation of circulating MM cells. © 2001 Cancer Research Campaign http://www.bjcancer.com
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页码:1387 / 1395
页数:8
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